Proszynski Tomasz J, Klemm Robin W, Gravert Maike, Hsu Peggy P, Gloor Yvonne, Wagner Jan, Kozak Karol, Grabner Hannes, Walzer Karen, Bagnat Michel, Simons Kai, Walch-Solimena Christiane
Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Proc Natl Acad Sci U S A. 2005 Dec 13;102(50):17981-6. doi: 10.1073/pnas.0509107102. Epub 2005 Dec 5.
Recently synthesized proteins are sorted at the trans-Golgi network into specialized routes for exocytosis. Surprisingly little is known about the underlying molecular machinery. Here, we present a visual screen to search for proteins involved in cargo sorting and vesicle formation. We expressed a GFP-tagged plasma membrane protein in the yeast deletion library and identified mutants with altered marker localization. This screen revealed a requirement of several enzymes regulating the synthesis of sphingolipids and ergosterol in the correct and efficient delivery of the marker protein to the cell surface. Additionally, we identified mutants regulating the actin cytoskeleton (Rvs161p and Vrp1p), known membrane traffic regulators (Kes1p and Chs5p), and several unknown genes. This visual screening method can now be used for different cargo proteins to search in a genome-wide fashion for machinery involved in post-Golgi sorting.
最近合成的蛋白质在反式高尔基体网络中被分类到专门的胞吐途径。令人惊讶的是,对于其潜在的分子机制知之甚少。在这里,我们展示了一种视觉筛选方法,用于寻找参与货物分类和囊泡形成的蛋白质。我们在酵母缺失文库中表达了一种带有绿色荧光蛋白标签的质膜蛋白,并鉴定出标记定位发生改变的突变体。该筛选揭示了几种调节鞘脂和麦角固醇合成的酶对于将标记蛋白正确且高效地递送至细胞表面是必需的。此外,我们还鉴定出了调节肌动蛋白细胞骨架的突变体(Rvs161p和Vrp1p)、已知的膜运输调节因子(Kes1p和Chs5p)以及几个未知基因。这种视觉筛选方法现在可用于不同的货物蛋白,以全基因组方式搜索参与高尔基体后分类的机制。